FDA 510(k)

CEREC Tessera基台块，CEREC Tessera基台系统

K号: K221402 · 2023-03-22

决定日期2023-03-22

产品代码NHA

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决定实质等同

器械摘要

CEREC Tessera Abutment Block, CEREC Tessera Abutment System is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2023-03-22 under 510(k) number K221402. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CEREC Tessera Abutment Block, CEREC Tessera Abutment System?

CEREC Tessera Abutment Block, CEREC Tessera Abutment System is a medical device that received FDA 510(k) clearance on 2023-03-22. The listed applicant is Dentsply Sirona, Inc.. The 510(k) number is K221402.

When did CEREC Tessera Abutment Block, CEREC Tessera Abutment System receive FDA 510(k) clearance?

CEREC Tessera Abutment Block, CEREC Tessera Abutment System received FDA 510(k) clearance on 2023-03-22, under 510(k) number K221402.

Who is the listed applicant for CEREC Tessera Abutment Block, CEREC Tessera Abutment System?

FDA 510(k)记录中列出Dentsply Sirona, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for CEREC Tessera Abutment Block, CEREC Tessera Abutment System?

The FDA product code for CEREC Tessera Abutment Block, CEREC Tessera Abutment System is NHA.

列明Dentsply Sirona, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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相关器械（代码：NHA）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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